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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704414Generated: October 30, 2026

beta-Phenylisovaleric acid → 3-Methyl-3-phenylbutan-1-ol

https://huagongshe.com/reaction/704414

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbeta-Phenylisovaleric acidHCID 13890—
ReactantHydrideHCID 166653—
ReactantSodium BicarbonateHCID 516892—
ReactantLithiumHCID 3028194—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-3-phenylbutan-1-olHCID 232460—

Reaction Steps

3-Methyl-3-phenylbutanoic acid (0.90 9) was dropwise added to a suspension of lithium alminum hydride (0.2 g) in 15 ml of tetrahydrofuran at room temperature and the mixture was stirred for 30 minutes. To the reaction mixture was added a saturated aqueous solution of sodium bicarbonate under ice cooling, and the reaction solution was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride,, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography (20 g). Elution with a hexane ethyl acetate (5:1) mixture gave 0.75 g of 3-metyl-3-phenylbutanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987132
Source datasetuspto-grants-1991_01
ORD IDord-f44441e6c92241f4803cf0b43b831589
Source noteuspto-grants-1991_01